U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 75

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901160copy number variation1nstd102humanBenign GRCh37 chr16: 84,228,873-84,230,500 , GRCh38.p12 chr16: 84,195,267-84,196,894 ADAD2, LOC654780
    nsv3921095copy number variation1nstd102humanPathogenic NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726 ADAD2, NECAB2, 219 more genes
    nsv3919844copy number variation1nstd102humanPathogenic GRCh38 chr16: 78,704,275-87,819,342 , GRCh37 chr16: 78,738,172-87,852,948 , NCBI36 chr16: 77,295,673-86,410,449 ADAD2, RPL10AP12, 146 more genes
    nsv3917609copy number variation1nstd102humanPathogenic NCBI36 chr16: 80,344,868-84,305,898 , GRCh37 chr16: 81,787,367-85,748,397 , GRCh38 chr16: 81,753,762-85,714,791 ADAD2, LOC105371376, 63 more genes
    nsv3911104copy number variation1nstd102humanPathogenic GRCh37 chr16: 83,912,597-87,257,444 , GRCh38 chr16: 83,878,992-87,223,838 , NCBI36 chr16: 82,470,098-85,814,945 ADAD2, LOC101928557, 75 more genes
    nsv3922440copy number variation1nstd102humanPathogenic NCBI36 chr16: 82,278,756-84,664,347 , GRCh37 chr16: 83,721,255-86,106,846 , GRCh38 chr16: 83,687,650-86,073,240 ADAD2, LOC123862, 58 more genes
    nsv3922490copy number variation1nstd102humanPathogenic GRCh38 chr16: 83,016,872-85,087,809 , GRCh37 chr16: 83,050,477-85,121,415 , NCBI36 chr16: 81,607,978-83,678,916 ADAD2, MBTPS1, 33 more genes
    nsv3922339copy number variation1nstd102humanPathogenic GRCh37 chr16: 83,432,665-84,941,726 , GRCh38 chr16: 83,399,060-84,908,120 , NCBI36 chr16: 81,990,166-83,499,227 ADAD2, LOC648774, 28 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 ADAD2, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 ADAD2, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 ADAD2, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 ADAD2, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 ADAD2, FTLP14, 1868 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 ADAD2, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ADAD2, ATMIN, 826 more genes
    nsv3915506copy number variation1nstd102humanPathogenic NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062 ADAD2, CFAP69P1, 716 more genes
    nsv3891306copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261 ADAD2, LOC107984894, 613 more genes
    nsv3913913copy number variation1nstd102humanPathogenic NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393 ADAD2, ATP5F1AP3, 534 more genes
    nsv3919817copy number variation1nstd102humanPathogenic NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985 ADAD2, LOC105376772, 527 more genes
    nsv3910304copy number variation1nstd102humanPathogenic NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403 ADAD2, MC1R, 528 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center